Job Summary
The Sr. Clinical Research Associate plays a crucial role in overseeing and managing clinical trials to ensure they are conducted in compliance with regulatory standards and the company’s protocols. This position is integral to the successful execution of clinical research projects, coordinating activities between the research sites and sponsors.
Responsibilities
- Monitor the progress of clinical trials, ensuring adherence to protocols and regulatory guidelines.
- Conduct site selection, initiation, monitoring, and closeout visits.
- Ensure data integrity and quality through thorough review and verification processes.
- Collaborate with cross-functional teams to facilitate the timely completion of studies.
- Provide training and support to site staff regarding trial protocols and procedures.
- Prepare and submit reports on trial progress and findings to stakeholders.
Qualifications
- Bachelor’s degree in Life Sciences or a related field; advanced degree preferred.
- Proven experience in clinical monitoring and knowledge of clinical trial management.
- Strong understanding of regulatory requirements and Good Clinical Practice (GCP).
- Excellent organizational, communication, and analytical skills.
- Ability to work independently and as part of a team in a fast-paced environment.
